Canonical Allele Identifier: CA2429833922

Gene: HSD17B10

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53432345C= , CM000685.2:g.53432345C=	GRCh38
NC_000023.10:g.53459293C= , CM000685.1:g.53459293C=	GRCh37
NC_000023.9:g.53476018C=	NCBI36
NG_008153.1:g.7031G= , LRG_450:g.7031G=
NG_033076.2:g.14491C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000495986.2:n.403G=
ENST00000682365.1:n.1594G=
ENST00000684251.1:n.103G=
ENST00000684503.1:n.424G=
ENST00000684692.1:c.259G=	ENSP00000506792.1:p.Val87=
ENST00000168216.11:c.259G= MANE Select	ENSP00000168216.6:p.Val87=
ENST00000168216.10:c.259G=	ENSP00000168216.6:p.Val87=
ENST00000375298.4:c.259G=	ENSP00000364447.4:p.Val87=
ENST00000375304.9:c.259G=	ENSP00000364453.5:p.Val87=
ENST00000495986.1:n.391G=
NM_001037811.2:c.259G= , LRG_450t2:c.259G=	NP_001032900.1:p.Val87=
NM_004493.2:c.259G= , LRG_450t1:c.259G=	NP_004484.1:p.Val87=
NM_004493.3:c.259G= MANE Select	NP_004484.1:p.Val87=